美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）

NDC包装代码	产品NDC	产品类型	商品名	通用名	剂型	给药途径	上市日期	结束日期	市场类别	申请号	标签持有者	活性成分	规格	包装描述
76420-010-30	76420-010	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20200123	N/A	ANDA	ANDA078722	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76420-010-30)
76420-010-60	76420-010	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20200123	N/A	ANDA	ANDA078722	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (76420-010-60)
76420-010-90	76420-010	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20221021	N/A	ANDA	ANDA078722	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (76420-010-90)
76420-019-30	76420-019	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20200604	N/A	ANDA	ANDA078722	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76420-019-30)
76420-019-60	76420-019	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20200604	N/A	ANDA	ANDA078722	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (76420-019-60)
76420-019-90	76420-019	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine Hydrochloride	Cyclobenzaprine Hydrochloride	TABLET, FILM COATED	ORAL	20200604	N/A	ANDA	ANDA078722	Asclemed USA, Inc.	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (76420-019-90)
85509-1001-6	85509-1001	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine HCL	Cyclobenzaprine HCL	TABLET, FILM COATED	ORAL	20250721	N/A	ANDA	ANDA078722	PHOENIX RX LLC	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (85509-1001-6)
85509-1001-9	85509-1001	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine HCL	Cyclobenzaprine HCL	TABLET, FILM COATED	ORAL	20250721	N/A	ANDA	ANDA078722	PHOENIX RX LLC	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (85509-1001-9)
85509-1001-1	85509-1001	HUMAN PRESCRIPTION DRUG	Cyclobenzaprine HCL	Cyclobenzaprine HCL	TABLET, FILM COATED	ORAL	20250721	N/A	ANDA	ANDA078722	PHOENIX RX LLC	CYCLOBENZAPRINE HYDROCHLORIDE	7.5 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (85509-1001-1)